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rs9977018

From SNPedia

Orientationplus
Stabilizedplus
Make rs9977018(G;G)
Make rs9977018(G;T)
Make rs9977018(T;T)
ReferenceGRCh38 38.1/141
Chromosome21
Position41616809
is asnp
is mentioned by
dbSNPrs9977018
ebirs9977018
HLIrs9977018
Exacrs9977018
Varsomers9977018
Maprs9977018
PheGenIrs9977018
hapmaprs9977018
1000 genomesrs9977018
hgdprs9977018
ensemblrs9977018
gopubmedrs9977018
geneviewrs9977018
scholarrs9977018
googlers9977018
pharmgkbrs9977018
gwascentralrs9977018
openSNPrs9977018
23andMers9977018
23andMe allrs9977018
SNP Nexus

SNPshotrs9977018
SNPdbers9977018
MSV3drs9977018
GWAS Ctlgrs9977018
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 24529757]
Trait Amyotrophic lateral sclerosis (sporadic)
Title A genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations.
Risk Allele
P-val 2E-9
Odds Ratio NR NR